A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6071338



Internal ID21980571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:74900712..74900712hg38UCSC Ensembl
chr3:74949863..74949863hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17542709
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6071338
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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